Evidence map›Paper›PMID 36374724›Full record

ArticleMolecular and biochemical parasitology2022

Application of a low-cost, specific, and sensitive loop-mediated isothermal amplification (LAMP) assay to detect Plasmodium falciparum imported from Africa.

Jiaqi Zhang, Xi Chen, Maohua Pan, Yucheng Qin, Hui Zhao, Qi Yang, Xinxin Li, Weilin Zeng, Zheng Xiang, Yanrui Wu and 11 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular and biochemical parasitology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Five Hot Topics in Tropical Medicine: 2025.Infectious disease reports · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 4 institutions in 3 countries.

Jiaqi ZhangDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China; Zhejiang Provincial Center for Disease Control and Prevention, No. 3399 BinSheng Road, Binjiang District, Hangzhou, Zhejiang Province 310051, China.
Xi ChenDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Maohua PanShanglin County People's Hospital, Shanglin, Guangxi 530500, China.
Yucheng QinShanglin County People's Hospital, Shanglin, Guangxi 530500, China.
Hui ZhaoDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Qi YangDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Xinxin LiDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Weilin ZengDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Zheng XiangDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Yanrui WuDepartment of Cell Biology & Genetics, Kunming Medical University, Kunming, Yunnan, China.
Mengxi DuanDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Xiaosong LiDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Xun WangDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Dominique MazierSorbonne Université, INSERM, CNRS, Centre d'Immunologie et des Maladies Infectieuses, CIMI, Paris, France.
Yanmei ZhangDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Wenya ZhuDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Kemin SunDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Yiman WuDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China.
Liwang CuiDepartment of Internal Medicine, Morsani College of Medicine, University of South Florida, 3720 Spectrum Boulevard, Suite 304, MDC84, Tampa, FL 33612, USA.
Yaming HuangDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China; Guangxi Zhuang Autonomous Region Center for Disease Prevention and Control, Nanning, Guangxi 530021, China. Electronic address: 1724501964@qq.com.
Zhaoqing YangDepartment of Pathogen Biology and Immunology, Kunming Medical University, Kunming, Yunnan 650500, China. Electronic address: yangzhaoqing@kmmu.edu.cn.
Kunming Medical University · CNSorbonne Université · FRUniversity of South Florida · USZhejiang Center for Disease Control and Prevention · CN

Funding

Southeast Asia Malaria Research CenterU19AI089672 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI CUI, LIWANG · 2010 to 2023
$28.9M
NIAID NIH HHS U19 AI089672
6 · The paper itself

Abstract

backgroundChinese citizens traveling abroad bring back imported malaria cases to China. Current malaria diagnostic tests, including microscopy and antigen-detecting rapid tests, cannot reliably detect low-density infections. To complement existing diagnostic methods, we aimed to develop a new loop-mediated isothermal amplification (LAMP) assay to detect and identify Plasmodium falciparum in Chinese travelers returning from Africa.

methodsWe developed a miniaturized LAMP assay to amplify the actin I gene of P. falciparum. Each reaction consumed only 25% of the reagents used in a conventional LAMP assay and the same amount of DNA templates used in nested PCR. We evaluated this LAMP assay's performance and compared it to microscopy and a nested PCR assay using 466 suspected malaria cases imported from Africa. We assessed the sensitivity of the new LAMP assay using cultured P. falciparum, clinical samples, and a plasmid construct, allowing unprecedented precision when quantifying the limit of detection.

resultsThe new LAMP assay was highly sensitive and detected two more malaria cases than nested PCR. Compared to nested PCR, the sensitivity and specificity of the novel LAMP assay were 100% [95% confidence interval (CI) 98.5-100%] and 99.1% (95% CI 96.7-99.9%), respectively. When evaluated using serial dilutions of the plasmid construct, the detection limit of the new LAMP was as low as 10

conclusionThe novel LAMP assay based on the P. falciparum actin I gene was specific, sensitive, and cost-effective, as it consumes 1/4 of the reagents in a typical LAMP reaction.

Indexed as

MalariaMalaria, FalciparumActinsAfricaHumansMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesPlasmodium falciparumSensitivity and SpecificityActinsCost-effective LAMPMalariaMolecular diagnosisPlasmodium falciparum

Identifiers

PMID36374724
PMCPMC9890345
OpenAlexW4307814966

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.